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Green-Light-Sensitive BODIPY Photoprotecting Groups for Amines

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journal contribution
posted on 25.01.2018, 00:00 by Kaja Sitkowska, Ben. L. Feringa, Wiktor Szymański
We describe a series of easily accessible, visible-light-sensitive (λ > 500 nm) BODIPY (boron-dipyrromethene)-based photoprotecting groups (PPGs) for primary and secondary amines, based on a carbamate linker. The caged compounds are stable under aqueous conditions for 24 h and can be efficiently uncaged in vitro with visible light (λ = 530 nm). These properties allow efficient photodeprotection of amines, rendering these novel PPGs potentially suitable for various applications, including the delivery of caged drugs and their remote activation.

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